rs794728633

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs794728633(A;A)

Make rs794728633(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64804443

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs794728633
dbSNP (classic)	rs794728633
ClinGen	rs794728633
ebi	rs794728633
HLI	rs794728633
Exac	rs794728633
Gnomad	rs794728633
Varsome	rs794728633
LitVar	rs794728633
Map	rs794728633
PheGenI	rs794728633
Biobank	rs794728633
1000 genomes	rs794728633
hgdp	rs794728633
ensembl	rs794728633
geneview	rs794728633
scholar	rs794728633
google	rs794728633
pharmgkb	rs794728633
gwascentral	rs794728633
openSNP	rs794728633
23andMe	rs794728633
SNPshot	rs794728633
SNPdbe	rs794728633
MSV3d	rs794728633
GWAS Ctlg	rs794728633

Max Magnitude

0

ClinVar
Risk	rs794728633(A;A)
Alt	rs794728633(A;A)
Reference	Rs794728633(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.64571915A>T
CLNSRC
CLNACC	RCV000182427.1,